A041702: A Randomized Phase III Study of Iburtinib Plus Obinutuzumab Versus Ibrutinib plus Venetoclax and Obinutuzumab in Untreated Older Patients (>70 Years of Age) with Chronic Lymphocytic Leukemia (CLL)
Aims: The purpose of this study is to discover if adding the drug Venetoclax will be better, the same or worse than the standard treatment and if stopping after 1 year of treatment is possible for those who have no detectable CLL.
Diagnosis: Chronic Lymphocytic Leukemia (CLL)
Principal investigator: David Grinblatt, MD
IRB Approval Number: EH19-149
Sponsor: Alliance for Clinical Trials in Oncology
Contact: Interested patients should contact research nurse Michele Britto, RN at 847.570.2109
Open to Enrollment: Yes
EAA173: Daratumumab to Enhance Therapeutic Effectiveness of Revlimid in Smoldering Myeloma (DETER-SMM)
Aims: The purpose of this study is to discover if adding the drug Venetoclax will be better, the same or worse than the standard treatment
Diagnosis: Smoldering Myeloma
Principal investigator: David Grinblatt, MD
IRB Approval Number: EH19-335
Sponsor: ECOG-ACRIN
Contact: Interested patients should contact research nurse Michele Britto, RN at 847.570.2109
Open to Enrollment: Yes
S1925:Randomized, Phase III Study of Early Intervention with Venetoclax and Obinutuzumab Versus Elayed Therapy with Venetoclas and Obinutuzumab in Newly Diagnosed Asymptomatic High-Risk Patients with Chronic Lymphyocytic Leukemia (CLL)/Small Lymphocytic Lymphoma (SLL): EVOLVE CLL/SLL Study
Aims: The purpose of this study is to compare starting treatment early versus starting treatment when you have symptoms in overall survival.
Diagnosis: Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma
Principal investigator: David Grinblatt, MD
IRB Approval Number: EH21-285
Sponsor: Southwest Oncology Group
Contact: Interested patients should contact research nurse Michele Britto, RN at 847.570.2109
Open to Enrollment: Yes
S1918: Phase II/III randomized study of R-miniCHOP with or without CC-486 (oral Azacitidine) in patients age 75 years or older wtih newly diagnosed diffuse large B-cell lymphoma, Grade IIIb follciular lymphoma, transformed lymphoma, and high-grade B-cell lymphomas with MYC and BCL2 and/or BCL6 rearrangements
Aims: The purpose of this study is to compare the addition of oral azacitidine to standard treatment.
Diagnosis: Large Cell Lymphoma
Principal investigator: Lynne Kaminer, MD
IRB Approval Number: EH22-044
Sponsor: Southwest oncology Group
Contact: Interested patients should contact research nurse Michele Britto at 847.570.2109
Open to Enrollment: Yes
EA9181: A Phase III Randomized Trial of Steroids + Tyrosine Kinase Inhibitor Induction with Chemotherapy or Blinatumomab for Newly Diagnosed BCR-ABL-positive Acute Lymphoblastic Leukemia in Adults
Aims: The purpose of this study is to compare using the use of chemotherapy versus blinatumomab in addition to steroids and tyrosine kinase inhibitor drugs as treatment.
Diagnosis: Acute Lymphoblastic Leukemia
Principal investigator: David Grinblatt, MD
IRB Approval Number: EH21-302
Sponsor: ECOG-ACRIN
Contact: Interested patients should contact research nurse Michele Britto, RN at 847.570.2109
Open to Enrollment: Yes
EA4181: A Randomized 3-Arm Phase II Study Comparing 1.) Bendamustine, Rituximab and High Dose Cytarabine (BR/CR) 2.) Bendamustine, Rituximab, High Dose Cytarabine and Acalabrutinib (BR/CR-A), and 3.) Bendamustine, Rituximab and Acalabrutinib (BR-A) in Patients <= 70 Years Old with Untreated Mantle Cell Lymphoma
Aims: The purpose of this study is to compare 3 drug regiments to see which is better or worse than the usual approach for mantle cell lymphoma
Diagnosis: Mantle Cell Lymphoma
Principal investigator: Amy Wang, MD
IRB Approval Number: EH22-092
Sponsor: ECOG-ACRIN
Contact: Interested patients should contact research nurse Michele Britto, RN at 847.570.2109
Open to Enrollment: Yes
A041501: A Phase III Trial to Evaluate the Efficacy of the Addition of Inotuzumab Ozogamicin (a Conjugated Anti-CD22 Monoclonal Antibody to Frontline Therapy in Young Adults (ages 18-39 years) with Newly Diagnosed Precursor B-Cell ALL.
Aims: The purpose of this study is to test the addition of an investigational drug, inotuzumab in addition to standard treatment for ALL.
Diagnosis: Acute Lymphocytic Leukemia (ALL)
Principal investigator: Lynne Kaminer, MD
IRB Approval Number: EH18-377
Sponsor: Alliance for Clinical Trials in Oncology
Contact: Interested patients should contact research nurse Michele Britto, RN at 847.570.2109
Open to Enrollment: Yes
Connect Myeloid: The myelofibrosis (MF), Myelodysplastic Syndromes (MDS) and Acute Myeloid Leukemia (AML Disease Registry
Aims: There are three main purposes of this study: 1. To use the information collected to help better understand patterns for diagnosis, treatment, and outcomes, including disease progression and survival. 2. To use the information to help better understand patterns for the quality of life in patients newly diagnosed with Lower-Risk, Higher-Risk, or unknown risk MDS or AML. 3. To use the results of this study to provide information to help better understand the effect different treatments have on a patient’s disease and on their quality of life.
Diagnosis: Myelodysplastic Syndrome (MDS) or Acute Myeloid Leukemia (AML)
Principal Investigator: Lynne Kaminer, MD
IRB Approval Number: EH13-390
Sponsor: Celgene, A Bristol Myers Squibb company
Contact: Interested patients should contact research nurse Michele Britto, RN at 847.570.2109
Open to Enrollment: Yes
A041701: A Randomized Phase II/III Study of Conventional Chemotherapy +/- Uproleselan (GMI-1271) in Older Adults with Acute Myeloid Leukemia Receiving Intenstive Induction Chemotherapy
Aims: The study is looking at whether we can lower the chance of the cancer returning if using Uproleselan in addition to standard of care drugs,
Diagnosis:Acute Myeloid Leukemia
Principal Investigator: David Grinblatt, MD
IRB Approval Number: EH21-284
Sponsor: Alliance for Clinical Trials in Oncology
Contact: Interested patients should contact research nurse Michele Britto, RN at 847.570.2109
Open to Enrollment: SUSPENDED
CIBMTR: Protocol for Research Database for Hematopoietic Cell Transplantation, Other Cellular Therapies and Marrow Toxic Injuries
Aims: The purpose of this study is to collect information on the collection of peripheral blood stem cells, transplant of stem cells, and the outcomes of patients who undergo peripheral blood stem cell transplant
Diagnosis: For patients undergoing a peripheral blood stem cell transplant
Principal Investigator: Lynne Kaminer, MD
IRB Approval Number: EH15-249
Sponsor: National Marrow Donor Program
Contact: Interested patients should contact research nurse Michele Britto, RN at 847.570.2109
Open to Enrollment: Yes